Teleflex ARROW GlideThru Manual page 2

A pdf copy of this IFU is located at www.teleflex.com/IFU
For a patient/user/third party in the European Union and in countries with identical
regulatory regime (Regulation 2017/745/EU on Medical Devices); if, during the use
of this device or as a result of its use, a serious incident has occurred, please report it to
the manufacturer and/or its authorized representative and to your national authority.
The contacts of national competent authorities (Vigilance Contact Points) and further
information can be found on the following European Commission website: https://
ec.europa.eu/growth/sectors/medical-devices/contacts_en
Symbol Glossary: Symbols are in compliance with ISO 15223-1.
Some symbols may not apply to this product. Refer to product labeling for symbols that apply specifically to this product.
Caution Medical device
Keep away Keep
from sunlight
Teleflex, the Teleflex logo, Arrow, the Arrow logo and GlideThru are trademarks or registered trademarks of Teleflex
Incorporated or its affiliates, in the U.S. and/or other countries. © 2020 Teleflex Incorporated. All rights reserved.
Importer
Consult
instructions for use
Do not use Not made
if package with natural
dry
is damaged rubber latex
Do not Do not
reuse resterilize
Catalogue
number
2
Sterilized by Single sterile barrier system with
ethylene oxide protective packaging inside
Lot
Use by
number
Single sterile
barrier system
Date of
Manufacturer
manufacture